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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 15 of 15 1 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants ... Nudel, Ron; Appadurai, Vivek; Buil, Alfonso. - : figshare, 2021 BASE Show details 2 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants ... Nudel, Ron; Appadurai, Vivek; Buil, Alfonso. - : figshare, 2021 BASE Show details 3 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants Nudel, Ron; Appadurai, Vivek; Buil, Alfonso... In: J Neurodev Disord (2021) BASE Show details 4 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study ... Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : figshare, 2020 BASE Show details 5 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study ... Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : figshare, 2020 BASE Show details 6 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica... In: BMC Neurosci (2020) BASE Show details 7 Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : John Wiley & Sons, Inc., 2019 BASE Show details 8 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 9 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry Andrea; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 10 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 11 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron. - : BioMed Central Ltd., 2016 BASE Show details 12 <The>> genetics of specific language impairment Nudel, Ron; Ceroni, Fabiola; Simpson, Nuala H.... In: Specific language impairment (Amsterdam, 2015), p. 7-34 MPI für Psycholinguistik Show details 13 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - 2015 BASE Show details 14 Associations of HLA alleles with specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - : BioMed Central, 2014 BASE Show details 15 Associations of HLA alleles with specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - 2014 BASE Show details

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